Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens

Detalhes bibliográficos
Autor(a) principal: Amorim,Marcelo R. de
Data de Publicação: 2018
Outros Autores: Hilário,Felipe, Sano,Paulo T., Bauab,Tais M., Santos,Lourdes C. dos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766
Resumo: The chemical investigation of ethyl acetate extract from Paepalanthus planifolius capitula resulted in the identification of 1H-naphtho[2,3-c]pyran-1-one,9-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-10-hydroxy-7-methoxy-3-methyl, semi-vioxanthin 9-O-β-D-glucopyranoside, toralactone-9-O-β-D-glucopyranoside, paepalantine-9-O-β-D-glucopyranoside, semi-vioxanthin, 1H-naphtho[2,3-c]pyran-1-one,3,4-dihydro-9,10-dihydroxy-5,7-dimethoxy-3-methyl, vioxanthin and paepalantine dimer, and also the isolation and identification of a new naphthopyranone dimer named planifoliusin A. The chemical structures of two compounds were elucidated by performing spectroscopic 1D and 2D nuclear magnetic resonance (NMR) experiments and spectrometric HRMS (high-resolution mass spectrometry) analysis. Other six naphthopyranone dimers were proposed by MS fragmentation patterns. The minimum inhibitory concentration (MIC) values for vioxanthin (7.8 µg mL-1), planifoliusin A (15.6 µg mL-1) and the ethyl acetate extract (31.2 µg mL-1) showed antimicrobial activity against Staphylococcus aureus (ATCC 25923).
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spelling Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human PathogensPaepalanthus planifoliusnaphthopyranoneantimicrobial activityThe chemical investigation of ethyl acetate extract from Paepalanthus planifolius capitula resulted in the identification of 1H-naphtho[2,3-c]pyran-1-one,9-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-10-hydroxy-7-methoxy-3-methyl, semi-vioxanthin 9-O-β-D-glucopyranoside, toralactone-9-O-β-D-glucopyranoside, paepalantine-9-O-β-D-glucopyranoside, semi-vioxanthin, 1H-naphtho[2,3-c]pyran-1-one,3,4-dihydro-9,10-dihydroxy-5,7-dimethoxy-3-methyl, vioxanthin and paepalantine dimer, and also the isolation and identification of a new naphthopyranone dimer named planifoliusin A. The chemical structures of two compounds were elucidated by performing spectroscopic 1D and 2D nuclear magnetic resonance (NMR) experiments and spectrometric HRMS (high-resolution mass spectrometry) analysis. Other six naphthopyranone dimers were proposed by MS fragmentation patterns. The minimum inhibitory concentration (MIC) values for vioxanthin (7.8 µg mL-1), planifoliusin A (15.6 µg mL-1) and the ethyl acetate extract (31.2 µg mL-1) showed antimicrobial activity against Staphylococcus aureus (ATCC 25923).Sociedade Brasileira de Química2018-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766Journal of the Brazilian Chemical Society v.29 n.4 2018reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20170199info:eu-repo/semantics/openAccessAmorim,Marcelo R. deHilário,FelipeSano,Paulo T.Bauab,Tais M.Santos,Lourdes C. doseng2018-03-12T00:00:00Zoai:scielo:S0103-50532018000400766Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2018-03-12T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
title Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
spellingShingle Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
Amorim,Marcelo R. de
Paepalanthus planifolius
naphthopyranone
antimicrobial activity
title_short Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
title_full Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
title_fullStr Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
title_full_unstemmed Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
title_sort Antimicrobial Activity of Paepalanthus planifolius and its Major Components against Selected Human Pathogens
author Amorim,Marcelo R. de
author_facet Amorim,Marcelo R. de
Hilário,Felipe
Sano,Paulo T.
Bauab,Tais M.
Santos,Lourdes C. dos
author_role author
author2 Hilário,Felipe
Sano,Paulo T.
Bauab,Tais M.
Santos,Lourdes C. dos
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Amorim,Marcelo R. de
Hilário,Felipe
Sano,Paulo T.
Bauab,Tais M.
Santos,Lourdes C. dos
dc.subject.por.fl_str_mv Paepalanthus planifolius
naphthopyranone
antimicrobial activity
topic Paepalanthus planifolius
naphthopyranone
antimicrobial activity
description The chemical investigation of ethyl acetate extract from Paepalanthus planifolius capitula resulted in the identification of 1H-naphtho[2,3-c]pyran-1-one,9-[(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-3,4-dihydro-10-hydroxy-7-methoxy-3-methyl, semi-vioxanthin 9-O-β-D-glucopyranoside, toralactone-9-O-β-D-glucopyranoside, paepalantine-9-O-β-D-glucopyranoside, semi-vioxanthin, 1H-naphtho[2,3-c]pyran-1-one,3,4-dihydro-9,10-dihydroxy-5,7-dimethoxy-3-methyl, vioxanthin and paepalantine dimer, and also the isolation and identification of a new naphthopyranone dimer named planifoliusin A. The chemical structures of two compounds were elucidated by performing spectroscopic 1D and 2D nuclear magnetic resonance (NMR) experiments and spectrometric HRMS (high-resolution mass spectrometry) analysis. Other six naphthopyranone dimers were proposed by MS fragmentation patterns. The minimum inhibitory concentration (MIC) values for vioxanthin (7.8 µg mL-1), planifoliusin A (15.6 µg mL-1) and the ethyl acetate extract (31.2 µg mL-1) showed antimicrobial activity against Staphylococcus aureus (ATCC 25923).
publishDate 2018
dc.date.none.fl_str_mv 2018-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532018000400766
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20170199
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.29 n.4 2018
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
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instname_str Sociedade Brasileira de Química (SBQ)
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reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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